1661
|
|
|
Cdk5 and Abl enzyme substrate 2 |
C20orf150, dJ908M14.2, ik3-2 |
|
1662
|
|
|
Calcium binding protein 1 |
CALBRAIN, HCALB_BR |
|
1663
|
|
|
Calcium binding protein 2 |
DFNB93 |
|
1664
|
|
|
Calcium binding protein 4 |
CRSD, CSNB2B |
Nocturnal frontal lobe epilepsy, Cone dystrophy, Cone-rod dystrophy, Cone-rod synaptic disorder, Congenital stationary night blindness, Night blindness, congenital stationary, Ocular albinism, Optic atrophy, Retinitis pigmentosa, Usher syndrome |
1665
|
|
|
Calcium binding protein 5 |
CABP3 |
|
1666
|
|
|
Calcium binding tyrosine phosphorylation regulated |
CABYRa, CABYRc, CABYRc/d, CABYRe, CBP86, CT88, FSP-2, FSP2 |
|
1667
|
|
|
Calcium channel flower domain containing 1 |
C9orf7, D9S2135, FLOWER |
|
1668
|
|
|
Calcium voltage-gated channel subunit alpha1 A |
APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2, EIEE42, FHM, HPCA, MHP, MHP1, SCA6 |
Alzheimer disease, Amyotrophic lateral sclerosis, Ataxia, Spinocerebellar ataxia, Auditory neuropathy, Benign paroxysmal torticollis of infancy, Bipolar disorder, Bulbar palsy, Cannabis abuse, Cerebellar ataxia, Cerebellar atrophy, Cerebral palsy, Chorea, Kidney disease, Color vision deficiency, Congenital neurologic anomalies, Cyclin-dependent kinase-like 5 deficiency, Vascular dementia, Developmental and epileptic encephalopathy, Dysarthria, Endometriosis, Absence epilepsy, Generalized epilepsy, Episodic ataxia, Gastroesophageal reflux disease, Global developmental delay, Gross motor development delay, Hemiplegic migraine, Intellectual developmental disorder, Lennox-gastaut syndrome, Major depressive disorder, Migraine, Neurodevelopmental disorder, Non-small cell lung carcinoma, Spastic ataxia, Strabismus, Substance abuseView all (22 more) |
1669
|
|
|
Calcium voltage-gated channel subunit alpha1 B |
BIII, CACNL1A5, CACNN, Cav2.2, DYT23, NEDNEH |
|
1670
|
|
|
Calcium voltage-gated channel subunit alpha1 C |
CACH2, CACN2, CACNA1C-IT2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, NEDHLSS, TS, TS. LQT8 |
Anhedonia, Anorexia nervosa, Anxiety disorder, Cardiac arrhythmias, Attention deficit hyperactivity disorder, Atypical femoral fracture, Timothy syndrome, Autism, Bipolar disorder, Brugada syndrome, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Cerebral palsy, Cognition disorder, Color vision deficiency, Concentric hypertrophic cardiomyopathy, Conduction disorder of the heart, Bipolar depression, Major depressive disorder, Epilepsy, Esophageal atresia, Long qt syndrome, Genetic predisposition to disease, Glomerulonephritis, Gout, Hypertension, Hypertrophic cardiomyopathy, Hypoglycemia, Inflammatory bowel disease, Intellectual developmental disorder, Congenital anomaly of limb, Metabolic syndrome, Mood disorder, Neurodevelopmental disorder, Non-organic psychosis, Non-specific syndromic intellectual disability, Obesity, Obsessive-compulsive disorder, Oligodendroglioma, Pancreatic cancer, Polymorphic catecholaminergic ventricular tachycardia, Psychiatric disorders, Psychotic disorders, Restrictive cardiomyopathy, Schizophrenia, Scoliosis, Short qt syndrome, Tetralogy of fallot, Tourette syndrome, Diabetes mellitus type 2, Ulcerative colitis, Depression, Ventricular fibrillation, Wolff-parkinson-white syndromeView all (40 more) |
